Expression and function of synaptotagmin VII in CTLs

被引:30
作者
Fowler, Kimberly T.
Andrews, Norma W.
Huleatt, James W.
机构
[1] Yale Univ, Sch Med, Sect Microbial Pathogenesis, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06510 USA
关键词
D O I
10.4049/jimmunol.178.3.1498
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Ca2+ sensor synaptotagmin (Syt) VII regulates the exocytosis of conventional lysosomes in several cell types. In CTLs, the Ca2+-regulated exocytosis of lytic granules/secretory lysosomes is responsible for the perforin/granzyme-mediated lysis of target cells. To investigate the role of Syt VII in CTL effector function, the expression and function of Syt VII were examined in wild-type and Syt VII-deficient mice. In comparison with Syt VII+/+ controls, Syt VII-/- animals were impaired in their ability to clear an infection with the intracellular pathogen Listeria monocytogenes. When isolated CTLs were examined, we found that Syt VII is expressed upon CTL activation and localizes to granzyme A-containing lytic granules. Syt VII-deficient CTLs have no defects in proliferation and cytokine production, and their lytic granules contain normal amounts of perforin and granzyme A and polarize normally at the immunological synapse. However, despite normal conjugate formation with target cells, CTLs from Syt VII-/- mice exhibit reduced effector activity, when compared with controls. Treatment of Syt VII+/+ or Syt VII-/- CTLs with an inhibitor of the perforin-mediated lytic pathway resulted in comparable levels of cytotoxic activity, suggesting that Syt VII regulates perforin-mediated cytolytic CTL responses.
引用
收藏
页码:1498 / 1504
页数:7
相关论文
共 41 条
[1]   Regulated secretion of conventional lysosomes [J].
Andrews, NW .
TRENDS IN CELL BIOLOGY, 2000, 10 (08) :316-321
[2]   There's more to life than neurotransmission: the regulation of exocytosis by synaptotagmin VII [J].
Andrews, NW ;
Chakrabarti, S .
TRENDS IN CELL BIOLOGY, 2005, 15 (11) :626-631
[3]  
BAETZ K, 1995, J IMMUNOL, V154, P6122
[4]   PIP2 increases the speed of response of synaptotagmin and steers its membrane-penetration activity toward the plasma membrane [J].
Bai, JH ;
Tucker, WC ;
Chapman, ER .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2004, 11 (01) :36-44
[5]   Synaptotagmin II negatively regulates Ca2+-triggered exocytosis of lysosomes in mast cells [J].
Baram, D ;
Adachi, R ;
Medalia, O ;
Tuvim, M ;
Dickey, BF ;
Mekori, YA ;
Sagi-Eisenberg, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (10) :1649-1657
[7]   Synaptotagmin isoforms couple distinct ranges of Ca2+, Ba2+, and Sr2+ concentration to SNARE-mediated membrane fusion [J].
Bhalla, A ;
Tucker, WC ;
Chapman, ER .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (10) :4755-4764
[8]   THE LYTIC GRANULES OF NATURAL-KILLER-CELLS ARE DUAL-FUNCTION ORGANELLES COMBINING SECRETORY AND PRE-LYSOSOMAL COMPARTMENTS [J].
BURKHARDT, JK ;
HESTER, S ;
LAPHAM, CK ;
ARGON, Y .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :2327-2340
[9]   The exocytosis-regulatory protein synaptotagminVII mediates cell invasion by Trypanosoma cruzi [J].
Caler, EV ;
Chakrabarti, S ;
Fowler, KT ;
Rao, S ;
Andrews, NW .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (09) :1097-1104
[10]   T-CELL RECEPTOR ALPHA-CHAIN PAIRING DETERMINES THE SPECIFICITY OF RESIDUE-262 WITHIN THE KB-RESTRICTED, OVALBUMIN257-264 DETERMINANT [J].
CARBONE, FR ;
STERRY, SJ ;
BUTLER, J ;
RODDA, S ;
MOORE, MW .
INTERNATIONAL IMMUNOLOGY, 1992, 4 (08) :861-867